Quality Engineer III — Medical Device (Onsite — Valencia, CA) Possible Contract Extension
On-siteValencia, California, United States
Job Summary
Lead failure investigations for return and non-return complaints on electro-mechanical medical devices by analyzing root causes, monitoring product performance trends, and escalating non-conformance issues. Create and validate test methods, work instructions, and SOPs while training technicians on sound failure analysis techniques. Review investigation results for accuracy and compliance, collaborate with R&D, Manufacturing, and Supplier teams to determine root causes, and present findings for SER/CRB. Own non-conformance investigations and champion cross-functional engineering initiatives to improve product performance and safety.
Required Qualifications
- Bachelor's degree in Electrical Engineering
- 4+ years of relevant experience
- Demonstrated problem-solving & failure analysis capabilities of electronics systems/components including those with RF communication
- Proficient with Microsoft Office tools including Word, Excel, PowerPoint, and Outlook
- Great written/verbal communication skills
- Ability to successfully multi-task and be adaptive
- Understanding of RF communication scheme/concepts
- Requires working in San Diego for a few months
Desired Qualifications
- Masters degree in Electrical Engineering
- 2-3 years experience in similar role
- Ability to understand system level functionalities, to devise and validate test methods for failure analysis of systems/components
- Experience in Medical Device industry
- Familiarity with Post Market requirements and systems
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.